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Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase
Tumor therapy needs new approaches in order to improve efficacy and reduce toxicity of the current treatments. The acidic microenvironment and the expression of high levels of endogenous non-telomerase reverse transcriptase (RT) are common features of malignant tumor cells. The anti-acidic proton pu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354819/ https://www.ncbi.nlm.nih.gov/pubmed/27926505 http://dx.doi.org/10.18632/oncotarget.13792 |
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author | Lugini, Luana Sciamanna, Ilaria Federici, Cristina Iessi, Elisabetta Spugnini, Enrico Pierluigi Fais, Stefano |
author_facet | Lugini, Luana Sciamanna, Ilaria Federici, Cristina Iessi, Elisabetta Spugnini, Enrico Pierluigi Fais, Stefano |
author_sort | Lugini, Luana |
collection | PubMed |
description | Tumor therapy needs new approaches in order to improve efficacy and reduce toxicity of the current treatments. The acidic microenvironment and the expression of high levels of endogenous non-telomerase reverse transcriptase (RT) are common features of malignant tumor cells. The anti-acidic proton pump inhibitor Lansoprazole (LAN) and the non-nucleoside RT inhibitor Efavirenz (EFV) have shown independent antitumor efficacy. LAN has shown to counteract drug tumor resistance. We tested the hypothesis that combination of LAN and EFV may improve the overall antitumor effects. We thus pretreated human metastatic melanoma cells with LAN and then with EFV, both in 2D and 3D spheroid models. We evaluated the treatment effect by proliferation and cell death/apoptosis assays in classical and in pulse administration experiments. The action of EFV was negatively affected by the tumor microenvironmental acidity, and LAN pretreatment overcame the problem. LAN potentiated the cytotoxicity of EFV to melanoma cells and, when administered during the drug interruption period, prevented the replacement of tumor cell growth. This study supports the implementation of the current therapies with combination of Proton Pumps and Reverse Transcriptase inhibitors. |
format | Online Article Text |
id | pubmed-5354819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53548192017-04-24 Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase Lugini, Luana Sciamanna, Ilaria Federici, Cristina Iessi, Elisabetta Spugnini, Enrico Pierluigi Fais, Stefano Oncotarget Research Paper Tumor therapy needs new approaches in order to improve efficacy and reduce toxicity of the current treatments. The acidic microenvironment and the expression of high levels of endogenous non-telomerase reverse transcriptase (RT) are common features of malignant tumor cells. The anti-acidic proton pump inhibitor Lansoprazole (LAN) and the non-nucleoside RT inhibitor Efavirenz (EFV) have shown independent antitumor efficacy. LAN has shown to counteract drug tumor resistance. We tested the hypothesis that combination of LAN and EFV may improve the overall antitumor effects. We thus pretreated human metastatic melanoma cells with LAN and then with EFV, both in 2D and 3D spheroid models. We evaluated the treatment effect by proliferation and cell death/apoptosis assays in classical and in pulse administration experiments. The action of EFV was negatively affected by the tumor microenvironmental acidity, and LAN pretreatment overcame the problem. LAN potentiated the cytotoxicity of EFV to melanoma cells and, when administered during the drug interruption period, prevented the replacement of tumor cell growth. This study supports the implementation of the current therapies with combination of Proton Pumps and Reverse Transcriptase inhibitors. Impact Journals LLC 2016-12-03 /pmc/articles/PMC5354819/ /pubmed/27926505 http://dx.doi.org/10.18632/oncotarget.13792 Text en Copyright: © 2017 Lugini et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Lugini, Luana Sciamanna, Ilaria Federici, Cristina Iessi, Elisabetta Spugnini, Enrico Pierluigi Fais, Stefano Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
title | Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
title_full | Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
title_fullStr | Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
title_full_unstemmed | Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
title_short | Antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
title_sort | antitumor effect of combination of the inhibitors of two new oncotargets: proton pumps and reverse transcriptase |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354819/ https://www.ncbi.nlm.nih.gov/pubmed/27926505 http://dx.doi.org/10.18632/oncotarget.13792 |
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